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Journal of Clinical Investigation, ISSN 0021-9738, 05/2015, Volume 125, Issue 5, pp. 1979 - 1986
Journal Article
Journal Article
Brain Research, ISSN 0006-8993, 2009, Volume 1265, pp. 158 - 170
Abstract Neurodegenerative diseases, such as Alzheimer's disease (AD) and Parkinson's disease (PD), are characterized by progressive loss of cognitive... 
Neurology | Neurodegenerative disease | Liquid chromatography with tandem mass spectrometry (LC–MS/MS) | Cerebrospinal fluid (CSF) | Two-dimensional gel electrophoresis (2-DE) | Neuronal pentraxin receptor (NPR) | Liquid chromatography with tandem mass spectrometry (LC-MS/MS) | CELL-ADHESION MOLECULE | ALZHEIMERS-DISEASE | BINDING PROTEIN 49 | RECOGNITION MOLECULES | SCHIZOPHRENIA | DYSTROGLYCAN | SYNAPTIC PLASTICITY | NEUROSCIENCES | N-CAM | EXPRESSION | PARKINSONS-DISEASE | Nerve Tissue Proteins - blood | Contactins | Humans | Middle Aged | Dipeptidases - cerebrospinal fluid | Electrophoresis, Gel, Two-Dimensional | Tandem Mass Spectrometry | C-Reactive Protein - metabolism | Contactin 2 | Neural Cell Adhesion Molecules - cerebrospinal fluid | Contactin 1 | Parkinson Disease - cerebrospinal fluid | Chromatography, Liquid | Cell Adhesion Molecules, Neuronal - cerebrospinal fluid | Cognition Disorders - cerebrospinal fluid | Protein Isoforms - cerebrospinal fluid | Nerve Tissue Proteins - cerebrospinal fluid | Alzheimer Disease - cerebrospinal fluid | C-Reactive Protein - cerebrospinal fluid | Blotting, Western | Nerve Tissue Proteins - metabolism | Dystroglycans - cerebrospinal fluid | Extracellular Matrix Proteins - cerebrospinal fluid | Cell Line, Tumor | Aged | Biomarkers - cerebrospinal fluid | Calcium-Binding Proteins - cerebrospinal fluid | Nervous system diseases | Cysteine | Neurons | Analysis | Amyloid beta-protein | Liquid chromatography | Public radio | Mass spectrometry | Alzheimer's disease
Journal Article
NeuroMolecular Medicine, ISSN 1535-1084, 03/2014, Volume 16, Issue 1, pp. 150 - 160
The success of future intervention strategies for Alzheimer's disease (AD) will likely rely on the development of treatments starting early in the disease... 
Cathepsins | TFEB | DRAM | hsc70 | PICALM | Proteasome | STANDARDIZATION | DEMENTIA | HUMAN CEREBROSPINAL-FLUID | AUTOPHAGY | MILD COGNITIVE IMPAIRMENT | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | PLASMA | DOWN-SYNDROME | UBIQUITIN PROTEASOME SYSTEM | EARLY ENDOSOMES | Lysosomal-Associated Membrane Protein 2 - cerebrospinal fluid | Phagosomes - chemistry | Lysosomes - chemistry | Lysosome-Associated Membrane Glycoproteins - cerebrospinal fluid | Humans | Middle Aged | Male | Microtubule-Associated Proteins - cerebrospinal fluid | Autophagy | rab GTP-Binding Proteins - cerebrospinal fluid | Aged, 80 and over | Amyloid beta-Peptides - cerebrospinal fluid | Adult | Albumins - cerebrospinal fluid | Female | Cerebrospinal Fluid Proteins - cerebrospinal fluid | Peptide Fragments - cerebrospinal fluid | Nerve Tissue Proteins - cerebrospinal fluid | tau Proteins - cerebrospinal fluid | Alzheimer Disease - cerebrospinal fluid | Vesicular Transport Proteins - cerebrospinal fluid | rab3 GTP-Binding Proteins - cerebrospinal fluid | Endosomes - chemistry | Aged | Biomarkers - cerebrospinal fluid | Neurosciences | Resveratrol | Amyloid beta-protein | Physiological aspects | Heat shock proteins | Brain damage | Development and progression | Biological markers | Alzheimer's disease | Membrane proteins | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | MEDICIN | Medicinska och farmaceutiska grundvetenskaper | PICALM; DRAM; TFEB; Cathepsins; Proteasome; hsc70 | Cell and Molecular Biology | MEDICINE | Cell- och molekylärbiologi
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 11/2015, Volume 86, Issue 11, pp. 1240 - 1247
BackgroundPatients presenting with parkinsonian syndromes share many clinical features, which can make diagnosis difficult. This is important as atypical... 
CRITERIA | SURGERY | PSYCHIATRY | CLINICAL-DIAGNOSIS | ALZHEIMERS-DISEASE | ALPHA-SYNUCLEIN | YKL-40 | CLINICAL NEUROLOGY | ACCURACY | MULTIPLE SYSTEM ATROPHY | RICHARDSON-OLSZEWSKI SYNDROME | RATING-SCALE | PROGRESSIVE SUPRANUCLEAR PALSY | Diagnosis, Differential | Parkinson Disease - pathology | Parkinsonian Disorders - cerebrospinal fluid | Prospective Studies | Supranuclear Palsy, Progressive - pathology | Multiple System Atrophy - pathology | Humans | Middle Aged | Parkinsonian Disorders - diagnosis | Nerve Tissue Proteins - cerebrospinal fluid | Male | Supranuclear Palsy, Progressive - cerebrospinal fluid | Multiple System Atrophy - cerebrospinal fluid | Parkinsonian Disorders - pathology | Parkinson Disease - cerebrospinal fluid | Dementia - cerebrospinal fluid | Parkinson Disease - diagnosis | Female | Aged | Biomarkers - cerebrospinal fluid | Multiple System Atrophy - diagnosis | Longitudinal Studies | Supranuclear Palsy, Progressive - diagnosis | Cohort Studies | Research | Cerebrospinal fluid | Diagnosis | Biological markers | Parkinsonism, Symptomatic | Risk factors | ykl-40 | Neurosciences | criteria | multiple | clinical-diagnosis | system atrophy | accuracy | alpha-synuclein | rating-scale | Surgery | richardson-olszewski syndrome | Psychiatry | Neurovetenskaper | progressive supranuclear palsy | alzheimers-disease
Journal Article
PLoS ONE, ISSN 1932-6203, 08/2015, Volume 10, Issue 8, p. e0135458
Journal Article
Neurology, ISSN 0028-3878, 2009, Volume 73, Issue 4, pp. 287 - 293
Journal Article
Psychiatry Research, ISSN 0165-1781, 07/2018, Volume 265, pp. 25 - 38
Over the last decade, finding a reliable biomarker for the early detection of schizophrenia (Scz) has been a topic of interest. The main goal of the current... 
SELENBP1 | GABA | Biomarker | Reelin | DISC1 | C-REACTIVE PROTEIN | DORSOLATERAL PREFRONTAL CORTEX | MESSENGER-RNA EXPRESSION | DTNBP1 DYSBINDIN GENE | PSYCHIATRY | OF-FUNCTION VARIANTS | NEUROTROPHIC-FACTOR | GROWTH-FACTOR LEVELS | DISCI | FACTOR VAL66MET POLYMORPHISM | INDUCED DOPAMINE RELEASE | LONG-TERM TREATMENT | Dysbindin - metabolism | Nerve Tissue Proteins - blood | Cell Adhesion Molecules, Neuronal - blood | Vascular Endothelial Growth Factor A | Catechol O-Methyltransferase - blood | Humans | Serine Endopeptidases - cerebrospinal fluid | Brain-Derived Neurotrophic Factor - blood | Nerve Growth Factors - metabolism | Brain - metabolism | Catechol O-Methyltransferase - metabolism | Nerve Growth Factors - cerebrospinal fluid | Brain-Derived Neurotrophic Factor - metabolism | Cell Adhesion Molecules, Neuronal - metabolism | Nerve Growth Factors - blood | Cell Adhesion Molecules, Neuronal - cerebrospinal fluid | Extracellular Matrix Proteins - metabolism | Biomarkers - metabolism | Schizophrenia - blood | Nerve Tissue Proteins - cerebrospinal fluid | Extracellular Matrix Proteins - blood | Biomarkers - blood | Schizophrenia - diagnostic imaging | Dysbindin - blood | Nerve Tissue Proteins - metabolism | Brain-Derived Neurotrophic Factor - cerebrospinal fluid | Extracellular Matrix Proteins - cerebrospinal fluid | Serine Endopeptidases - blood | Dysbindin - cerebrospinal fluid | Prefrontal Cortex - metabolism | Serine Endopeptidases - metabolism | Biomarkers - cerebrospinal fluid | Catechol O-Methyltransferase - cerebrospinal fluid | Schizophrenia - cerebrospinal fluid | Tyrosine | Medical research | Neurosciences | Endothelial growth factors | RNA | Glycogen | HLA histocompatibility antigens | Schizophrenia | Nerve growth factor | Glutamate decarboxylase | Glutamate | Muscle proteins | Anopheles | Synthesis | Histocompatibility antigens | Interleukins | Medicine, Experimental | Selenium | Biological markers | Protein binding
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2016, Volume 6, Issue 1, p. 38305
Mucopolysaccharidosis (MPS) type-IH is a lysosomal storage disease that results from mutations in the IDUA gene causing the accumulation of glycosaminoglycans... 
HURLER-SYNDROME | ENZYME REPLACEMENT | OPENING PRESSURE | THERAPY | MULTIDISCIPLINARY SCIENCES | TRANSPLANT | TNF-ALPHA | BONE | CEREBROSPINAL-FLUID | REFERENCE RANGE | DELIVERY | Interleukin-8 - genetics | Mucopolysaccharidosis I - cerebrospinal fluid | Humans | Child, Preschool | Infant | Interleukin-8 - cerebrospinal fluid | Male | Glucose - cerebrospinal fluid | Chemokine CXCL12 - cerebrospinal fluid | Adaptor Proteins, Signal Transducing - cerebrospinal fluid | Chemokine CCL2 - cerebrospinal fluid | Heparitin Sulfate - cerebrospinal fluid | Chemokine CXCL12 - genetics | Iduronidase - cerebrospinal fluid | Female | Child | Iduronidase - genetics | Iduronidase - deficiency | Gene Expression | Mucopolysaccharidosis I - pathology | Nerve Tissue Proteins - cerebrospinal fluid | Chemokine CCL2 - genetics | Nerve Tissue Proteins - genetics | Cerebrospinal Fluid Pressure | Mucopolysaccharidosis I - diagnosis | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Mucopolysaccharidosis I - genetics | Biomarkers - cerebrospinal fluid | Mutation | Heparan sulfate | Glycosaminoglycans | Mucopolysaccharidosis | Inflammation | Cerebrospinal fluid | SDF-1 protein | IDUA gene | Neurodegeneration | Biomarkers | Children | Sulfate | Vascular endothelial growth factor | Macrophage inflammatory protein | Monocyte chemoattractant protein 1 | Interleukin 8
Journal Article